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Super Sunnies lavender flex

by Lucas Specialty Products

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850862001901 UDI-DI Date21 Aug 2023ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Super Sunnies
Generic Name
Non-prescription sunglasses
Model / Reference
lavender flex
Primary DI / UDI-DI
00850862001901
FDA Product Code
IWS
GMDN Term
Non-prescription sunglasses
Device Class
Class I
Regulation Number
892.6500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Tinted non-prescription spectacles

Other devices from Lucas Specialty Products

See all devices from Lucas Specialty Products →

Properties

  • Premarket Exempt

Other properties (13)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No